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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
To sell food and drink products, the label must be: clear and easy to read…
You must show the following information: the name of the food a ‘best…
If your food or drink product has 2 or more ingredients (including any…
You must show an appropriate warning on the label if your food contains…
Nutrition labelling You must follow nutrition labelling information rules…
If you’re a retailer, you can label products ‘organic’ as long as: at…
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Explains how conditions attached to a planning permission should be used and discharged effectively
Find out if a claim of ownership by adverse possession can be made on common land and town or village greens, what effect it will have on the land and whether a claim can be opposed.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Application form ADV1: registration of a person in adverse possession.
Guidance on adverse possession where a right to be registered was acquired before 13 October 2003 (practice guide 5).
Device-specific guidance for manufacturers on reporting adverse incidents under the vigilance system
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